美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
76420-665-30	76420-665	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	.5 mg/1	30 TABLET in 1 BOTTLE (76420-665-30)
76420-665-60	76420-665	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	.5 mg/1	60 TABLET in 1 BOTTLE (76420-665-60)
76420-665-90	76420-665	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	.5 mg/1	90 TABLET in 1 BOTTLE (76420-665-90)
76420-666-01	76420-666	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	2 mg/1	100 TABLET in 1 BOTTLE (76420-666-01)
76420-666-30	76420-666	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	2 mg/1	30 TABLET in 1 BOTTLE (76420-666-30)
76420-666-60	76420-666	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	2 mg/1	60 TABLET in 1 BOTTLE (76420-666-60)
76420-666-90	76420-666	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20240111	N/A	NDA AUTHORIZED GENERIC	NDA018276	Asclemed USA, Inc.	ALPRAZOLAM	2 mg/1	90 TABLET in 1 BOTTLE (76420-666-90)
82804-027-30	82804-027	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20231023	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.25 mg/1	30 TABLET in 1 BOTTLE (82804-027-30)
82804-027-60	82804-027	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20231023	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.25 mg/1	60 TABLET in 1 BOTTLE (82804-027-60)
82804-027-90	82804-027	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20231023	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.25 mg/1	90 TABLET in 1 BOTTLE (82804-027-90)
63187-971-30	63187-971	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20180101	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	2 mg/1	30 TABLET in 1 BOTTLE (63187-971-30)
63187-971-60	63187-971	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20180101	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	2 mg/1	60 TABLET in 1 BOTTLE (63187-971-60)
63187-971-90	63187-971	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20180101	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	2 mg/1	90 TABLET in 1 BOTTLE (63187-971-90)
71205-614-02	71205-614	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20211015	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	1 mg/1	2 TABLET in 1 BOTTLE (71205-614-02)
71205-614-30	71205-614	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20211015	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	1 mg/1	30 TABLET in 1 BOTTLE (71205-614-30)
71205-614-60	71205-614	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20211015	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	1 mg/1	60 TABLET in 1 BOTTLE (71205-614-60)
71205-614-90	71205-614	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20211015	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	1 mg/1	90 TABLET in 1 BOTTLE (71205-614-90)
71205-652-30	71205-652	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20220412	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.5 mg/1	30 TABLET in 1 BOTTLE (71205-652-30)
71205-652-60	71205-652	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20220412	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.5 mg/1	60 TABLET in 1 BOTTLE (71205-652-60)
71205-652-90	71205-652	HUMAN PRESCRIPTION DRUG	Alprazolam	alprazolam	TABLET	ORAL	20220412	N/A	NDA AUTHORIZED GENERIC	NDA018276	Proficient Rx LP	ALPRAZOLAM	.5 mg/1	90 TABLET in 1 BOTTLE (71205-652-90)